Programmed Cell Death Pathways in Cholangiocarcinoma: Opportunities for Targeted Therapy.

apoptosis cholangiocarcinoma ferroptosis necroptosis programmed cell death pyroptosis targeted therapy

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
15 Jul 2023
Historique:
received: 16 05 2023
revised: 06 07 2023
accepted: 12 07 2023
medline: 29 7 2023
pubmed: 29 7 2023
entrez: 29 7 2023
Statut: epublish

Résumé

Cholangiocarcinoma is a highly aggressive cancer arising from the bile ducts. The limited effectiveness of conventional therapies has prompted the search for new approaches to target this disease. Recent evidence suggests that distinct programmed cell death mechanisms, namely, apoptosis, ferroptosis, pyroptosis and necroptosis, play a critical role in the development and progression of cholangiocarcinoma. This review aims to summarize the current knowledge on the role of programmed cell death in cholangiocarcinoma and its potential implications for the development of novel therapies. Several studies have shown that the dysregulation of apoptotic signaling pathways contributes to cholangiocarcinoma tumorigenesis and resistance to treatment. Similarly, ferroptosis, pyroptosis and necroptosis, which are pro-inflammatory forms of cell death, have been implicated in promoting immune cell recruitment and activation, thus enhancing the antitumor immune response. Moreover, recent studies have suggested that targeting cell death pathways could sensitize cholangiocarcinoma cells to chemotherapy and immunotherapy. In conclusion, programmed cell death represents a relevant molecular mechanism of pathogenesis in cholangiocarcinoma, and further research is needed to fully elucidate the underlying details and possibly identify therapeutic strategies.

Identifiants

pubmed: 37509299
pii: cancers15143638
doi: 10.3390/cancers15143638
pmc: PMC10377326
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Subventions

Organisme : Min Salute-PNRR
ID : PNC-E3-2022-23683266 PNCHLS-DA
Organisme : Italian Association for Cancer Research
ID : IG 2022 ID 27366; 2023-2027
Organisme : Italian Association for Cancer Research
ID : IG#22206; 2019-2023

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Auteurs

Manuel Scimeca (M)

Department of Experimental Medicine, TOR, University of Rome Tor Vergata, 00133 Rome, Italy.

Valentina Rovella (V)

Department of Systems Medicine, University of Rome Tor Vergata, 00133 Rome, Italy.

Valeria Palumbo (V)

Department of Experimental Medicine, TOR, University of Rome Tor Vergata, 00133 Rome, Italy.

Maria Paola Scioli (MP)

Department of Experimental Medicine, TOR, University of Rome Tor Vergata, 00133 Rome, Italy.

Rita Bonfiglio (R)

Department of Experimental Medicine, TOR, University of Rome Tor Vergata, 00133 Rome, Italy.

Gerry Melino (G)

Department of Experimental Medicine, TOR, University of Rome Tor Vergata, 00133 Rome, Italy.

Mauro Piacentini (M)

Department of Biology, University of Rome Tor Vergata, 00133 Rome, Italy.

Luigi Frati (L)

Institute Pasteur Italy-Cenci Bolognetti Foundation, Via Regina Elena 291, 00161 Rome, Italy.
IRCCS Neuromed S.p.A., Via Atinense 18, 86077 Pozzilli, Italy.

Massimiliano Agostini (M)

Department of Experimental Medicine, TOR, University of Rome Tor Vergata, 00133 Rome, Italy.

Eleonora Candi (E)

Department of Experimental Medicine, TOR, University of Rome Tor Vergata, 00133 Rome, Italy.

Alessandro Mauriello (A)

Department of Experimental Medicine, TOR, University of Rome Tor Vergata, 00133 Rome, Italy.

Classifications MeSH